Evidence map›Paper›PMID 40956833›Full record

ArticlePloS one2025

Optimized processing of Gardenia Fruits with ginger juice: Unveiling therapeutic mechanisms for cholestatic liver injury through TLR4/NF-κB, FXR/PPAR-α, and PI3K/AKT/GSK-3β.

Chenzi Lyu, Xianglong Meng, Juan Wang, Haifeng Shao, Yang Wang, Yong-Ki Park, Shuosheng Zhang, Hyo Won Jung

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Chenzi LyuDepartment of Herbology, College of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.ORCID https://orcid.org/0000-0002-0668-1447
Xianglong MengCollege of Chinese Materia Medica and Food Engineering, Shanxi University of Chinese Medicine, Jinzhong, Shanxi, China.
Juan WangCollege of Chinese Materia Medica and Food Engineering, Shanxi University of Chinese Medicine, Jinzhong, Shanxi, China.
Haifeng ShaoDepartment of Herbology, College of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.ORCID https://orcid.org/0000-0002-6982-9277
Yang WangDepartment of Herbology, College of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.ORCID https://orcid.org/0009-0008-0998-9552
Yong-Ki ParkDepartment of Herbology, College of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.
Shuosheng ZhangCollege of Chinese Materia Medica and Food Engineering, Shanxi University of Chinese Medicine, Jinzhong, Shanxi, China.
Hyo Won JungDepartment of Herbology, College of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.ORCID https://orcid.org/0000-0002-3623-5528

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study aimed to optimize the processing conditions of Gardeniae Fructus with ginger juice (GFPG) and confirm its therapeutic effects and pharmacological mechanisms on cholestatic liver injury. Processing conditions were optimized using response surface methodology (RSM) and thermal analysis, focusing on geniposide content as a key active compound. Variables included processing time, moistening time, and the solid-liquid ratio. Optimal conditions were: ginger juice to Gardeniae Fructus ratio of 8:1 (w/v), processing temperature of 208 °C, moistening time of 3 hours, and processing time of 5 minutes. Pharmacological mechanisms were analyzed through network pharmacology, molecular docking, and experimental validation using alpha-naphthyl isothiocyanate (ANIT)-induced cholestatic liver injury in mice and lipopolysaccharide (LPS)-stimulated RAW264.7 cell models. In vivo, GFPG extract alleviated ANIT-induced cholestatic liver injury by improving liver function markers (AST, ALT, TBA, TBIL, DBIL) and modulating TLR4/NF-κB, FXR/PPAR-α, and PI3K/AKT/GSK-3β pathways. In vitro, it reduced LPS-induced production of inflammatory mediators (NO, TNF-α, IL-6, IL-1β) through TLR4/NF-κB pathway inhibition. This study established optimal processing methods for GFPG using RSM and thermal analysis, providing robust quantitative parameters. GFPG demonstrated significant therapeutic effects in cholestatic liver injury models, indicating its potential as a candidate for developing treatments for cholestatic hepatitis.

Indexed as

CholestasisGardeniaPlant ExtractsZingiber officinale1-NaphthylisothiocyanateAnimalsFruitGlycogen Synthase Kinase 3 betaLipopolysaccharidesLiverMaleMiceMolecular Docking SimulationNF-kappa BPhosphatidylinositol 3-KinasesPPAR alpha1-NaphthylisothiocyanateGlycogen Synthase Kinase 3 betaLipopolysaccharidesNF-kappa BPhosphatidylinositol 3-KinasesPlant ExtractsPPAR alphaProto-Oncogene Proteins c-aktReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID40956833
PMCPMC12440179

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.